Specialist, Quality Document Control
Rocket Pharmaceuticals
6 months ago
On-site
Cranbury, NJ
Operations
Position Summary:
The Specialist, Quality Document Control will support the management and control of documentation at Rocket, including within the ZenQMS electronic quality system. The role manages all paper-based documents and records and is the primary owner of the document control storage room for paper records/logbooks, batch records, etc.
Responsibilities:
- Manage documents within the ZenQMS electronic quality system.
- Issue and archive paper-based documents and records, including batch records, logbooks, and controlled forms.
- Oversee and manage the on-site physical document storage room.
- Support functional groups in managing their documents.
- Support the ZenQMS team in managing documents within the system.
Qualifications:
- Associate’s Degree in a science-related field (preferred).
- Minimum 3 years of experience in a document control or document management role.
- Experience with electronic document management systems (ZenQMS, Veeva, etc.).
- Minimum 3–5 years of quality biopharma experience.
- Familiarity with standard software (Microsoft Word, Excel, PowerPoint, etc.).
- Ability to work within a multifunctional team.
- Ability to work with documents, including pushing carts to transport batch records and large document/binder sets.
Compensation/Benefits (as stated):
- Expected salary range: $56,000 to $68,000.
The Specialist, Quality Document Control will support the management and control of documentation at Rocket, including within the ZenQMS electronic quality system. The role manages all paper-based documents and records and is the primary owner of the document control storage room for paper records/logbooks, batch records, etc.
Responsibilities:
- Manage documents within the ZenQMS electronic quality system.
- Issue and archive paper-based documents and records, including batch records, logbooks, and controlled forms.
- Oversee and manage the on-site physical document storage room.
- Support functional groups in managing their documents.
- Support the ZenQMS team in managing documents within the system.
Qualifications:
- Associate’s Degree in a science-related field (preferred).
- Minimum 3 years of experience in a document control or document management role.
- Experience with electronic document management systems (ZenQMS, Veeva, etc.).
- Minimum 3–5 years of quality biopharma experience.
- Familiarity with standard software (Microsoft Word, Excel, PowerPoint, etc.).
- Ability to work within a multifunctional team.
- Ability to work with documents, including pushing carts to transport batch records and large document/binder sets.
Compensation/Benefits (as stated):
- Expected salary range: $56,000 to $68,000.